利用冶金渣作为铁源直接形成柠檬酸铁络合物,通过光-芬顿工艺去除微污染物

Catalysts Pub Date : 2024-07-04 DOI:10.3390/catal14070426
Sandra Yazmin Arzate Salgado, Ana Yañez-Aulestia, Rosa-María Ramírez-Zamora
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摘要

按照循环经济的目标,这项工作证明了工业副产品可用于环境修复。通过同时进行铁的活化和螯合阶段,利用冶金渣和柠檬酸形成了铁与柠檬的复合物,铁的回收率达到 87%。在光-芬顿过程中对该复合物进行了评估,通过水杨酸剂量测定或水杨酸羟基化反应产生 HO-,运行 30 分钟后产生 0.13 ± 0.1 mM HO-;该值比报告的冶金渣(作为异相催化剂,22 μM)在类似光-芬顿过程中的值高出三个数量级。测试了该系统降解药物混合物的能力,包括地塞米松(DEX)、萘普生(NAP)和酮咯酸(KTR),这些药物通常用于治疗 COVID-19 的症状。药物降解测试分两个阶段进行。在第一阶段,将冶金渣中的 Fe:Cit 复合物与分析级反应物形成的复合物进行比较;前者的药物降解速度更快,在 5 厘米和 500 W/m2 的条件下观察到的主要差异更大。在这里,使用矿渣中的 Fe:Cit 在 5 分钟内就降解了 85-90% 的药物,而使用分析试剂至少需要 20 分钟才能达到这种降解效果,这可能是因为矿渣中的痕量化合物被活化的缘故。然后,测试了液体深度(5、10 和 15 厘米)和辐照度(250、500 和 750 瓦/平方米)的影响;三种模型污染物的假一阶动力学降解常数范围为 0.009 > kD > 0.09 min-1,这表明 DEX 的降解比 NAP 和 KRT 更可行,因为自由基攻击的可行性与分子结构有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Direct Formation of an Iron Citrate Complex Using a Metallurgical Slag as an Iron Source for Micropollutant Removal via the Photo-Fenton Process
Following the goals of the circular economy, this work demonstrates that an industrial by-product can be used in environmental remediation. Metallurgical slag and citric acid were used to form an Fe:Cit complex by simultaneously carrying out the lixiviation of the iron and the chelating stages with an 87% iron recovery. This complex was evaluated in the photo-Fenton process to produce HO• through salicylic acid dosimetry or salicylic acid hydroxylation, producing 0.13 ± 0.1 mM HO• after 30 min of operation; such a value is three orders of magnitude higher than the one reported for the metallurgical slag (as a heterogeneous catalyst, 22 μM) in the photo-Fenton-like process. The system was tested for its ability to degrade a mixture of drugs, including dexamethasone (DEX), naproxen (NAP), and ketorolac (KTR), which are often used to treat the symptoms of COVID-19. The drug degradation tests were performed in two stages. In the first stage, the Fe:Cit complex from the metallurgical slag was compared to the one formed by analytical-grade reactants; the drug degradation was faster for the former, with the major difference being observed at 5 cm and 500 W/m2. Here, 85–90% of the drugs was degraded in 5 min using Fe:Cit from slag, while at least 20 min was necessary to achieve such degradation with the analytical reagent, conceivably because of the trace compounds being lixiviated from the slag. Then, the effects of the liquid depth (5, 10, and 15 cm) and irradiance (250, 500, and 750 W/m2) were tested; the pseudo-first-order kinetic degradation constants for the three model pollutants were in the range of 0.009 > kD > 0.09 min−1, showing that degradation is more feasible for DEX than for NAP and KRT because the radical attack feasibility is related to the molecular structures.
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